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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37116Erstellt: 23. Oktober 2026

p-Toluenesulfonic acid → 6-cyano-3,4-dihydro-2,2-dimethyl-4-(6-oxo-1-cyclohexen-1-yl)-2H-1,4-benzoxazine

https://huagongshe.com/de/reaction/37116

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acidHCID 6101—
Edukt1,2-CyclohexanedioneHCID 13006—
Edukt6-cyano-3,4-dihydro-2,2-dimethyl-2H-1,4-benzoxazineHCID 10535622—
LösungsmittelTolueneHCID 1140—
Produkt6-cyano-3,4-dihydro-2,2-dimethyl-4-(6-oxo-1-cyclohexen-1-yl)-2H-1,4-benzoxazineHCID 1049316566,7%

Reaktionsschritte

In 15 ml of toluene were dissolved 0.5 g of 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1,4-benzoxazine, 0.33 g of cyclohexane-1,2-dione and a catalytic amount of p-toluenesulfonic acid and using a Dean-Stark trap, the solution was refluxed under heating for 4 hours. After cooling, the reaction mixture was washed with saturated aqueous sodium hydrogen carbonate solution and aqueous sodium chloride solution and dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography and the resulting crude crystals were washed with ethanol to give 0.5 g of 6-cyano-3,4-dihydro-2,2-dimethyl-4-(6-oxo-1-cyclohexen-1-yl)-2H-1,4-benzoxazine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05420126
Quelldatensatzuspto-grants-1995_05
ORD IDord-543880f311e840e5a659f21d25f74264
Quellennotizuspto-grants-1995_05